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3-phenyl-1,5,6,7-tetrahydro-indol-4-one is a complex organic compound with a molecular formula of C14H15NO. It is a derivative of indole, a heterocyclic aromatic organic compound that contains a benzene ring fused to a pyrrole ring. This specific compound features a phenyl group (a benzene ring with a hydrogen atom replaced by a carbon-carbon double bond) attached to the indole structure at the 3-position, and a carbonyl group (C=O) at the 4-position. The compound is characterized by its tetrahydro nature, indicating that it has four hydrogen atoms added across a double bond, which in this case, affects the indole ring structure. This chemical is of interest in the field of organic chemistry and may have potential applications in the synthesis of pharmaceuticals or other chemical products due to its unique structure and properties.

6577-97-5

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6577-97-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6577-97-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,5,7 and 7 respectively; the second part has 2 digits, 9 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 6577-97:
(6*6)+(5*5)+(4*7)+(3*7)+(2*9)+(1*7)=135
135 % 10 = 5
So 6577-97-5 is a valid CAS Registry Number.

6577-97-5Downstream Products

6577-97-5Relevant academic research and scientific papers

Efficient synthesis of pyrroles and 4,5,6,7-tetrahydroindoles via palladium-catalyzed oxidation of hydroxy-enamines

Aoyagi, Yutaka,Mizusaki, Toshihiko,Shishikura, Masahiro,Komine, Takashi,Yoshinaga, Tokuji,Inaba, Haruko,Ohta, Akihiro,Takeya, Koichi

, p. 8533 - 8538 (2007/10/03)

Facile and one-pot synthetic route of poly-substituted pyrroles and 4-oxo-4,5,6,7-tetrahydroindoles is established, which consists of three steps: (1) palladium-catalyzed oxidation of hydroxy-enamines by using tetrakis(triphenylphosphine)palladium and mesityl bromide oxidation system, (2) intramolecular cyclization, and (3) dehydration.

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